原发性硬化性胆管炎
炎症性肠病
肠道菌群
发病机制
遗传倾向
医学
肝病
疾病
串扰
免疫学
胃肠病学
内科学
光学
物理
作者
You Sun Kim,Edward Hurley,Yoojeong Park,Sungjin Ko
标识
DOI:10.1038/s12276-023-01042-9
摘要
Abstract The close relationship between primary sclerosing cholangitis (PSC) and inflammatory bowel disease (IBD) provides a good opportunity to comprehend the gut–liver axis. The gut and the liver have reciprocal interactions, including how gut inflammation influences the liver through immune cells and the microbiota and how the microbiota in the gut modifies bile acids, which are produced and secreted from the liver. PSC-IBD shows distinct clinical findings from classical IBD. In addition, a distinct genetic predisposition and unique microbiota composition suggest that PSC-IBD is an independent disease entity. Understanding the pathogenesis of PSC-IBD helps to develop novel and effective therapeutic agents. Given the high risk of malignancies associated with PSC-IBD, it is critical to identify patients at high risk and implement appropriate surveillance and monitoring strategies. In this review, we provide an overview of PSC-IBD, which exemplifies the gut–liver axis.
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